Affinity DataIC50: 11nMAssay Description:Inhibition of Grb2 by ELISAMore data for this Ligand-Target Pair
Affinity DataIC50: 11nMAssay Description:The compound was evaluated for its potency to inhibit the interaction between Growth factor receptor bound protein 2 and phosphotyrosine-containing p...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Affinity DataIC50: 50nMAssay Description:Antagonist activity at rat TRPV1 expressed in Xenopus laevis oocytes assessed as blockage of capsaicin-induced current at holding potential -60 mV by...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Affinity DataIC50: 100nMAssay Description:Antagonist activity at rat TRPV1 expressed in Xenopus laevis oocytes assessed as blockage of capsaicin-induced current at holding potential -60 mV by...More data for this Ligand-Target Pair
Affinity DataIC50: 120nMAssay Description:The compound was evaluated for its potency to inhibit the interaction between Growth factor receptor bound protein 2 and phosphotyrosine-containing p...More data for this Ligand-Target Pair
Affinity DataIC50: 153nMAssay Description:The compound was evaluated for its potency to inhibit the interaction between Growth factor receptor bound protein 2 and phosphotyrosine-containing p...More data for this Ligand-Target Pair
Affinity DataIC50: 198nMAssay Description:The compound was evaluated for its potency to inhibit the interaction between Growth factor receptor bound protein 2 and phosphotyrosine-containing p...More data for this Ligand-Target Pair
Affinity DataIC50: 235nMAssay Description:The compound was evaluated for its potency to inhibit the interaction between Growth factor receptor bound protein 2 and phosphotyrosine-containing p...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Affinity DataIC50: 300nMAssay Description:Antagonist activity at rat TRPV1 expressed in Xenopus laevis oocytes assessed as blockage of capsaicin-induced current at holding potential -60 mV by...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Affinity DataIC50: 450nMAssay Description:Antagonist activity at rat TRPV1 expressed in Xenopus laevis oocytes assessed as blockage of capsaicin-induced current at holding potential -60 mV by...More data for this Ligand-Target Pair
Affinity DataIC50: 497nMAssay Description:The compound was evaluated for its potency to inhibit the interaction between Growth factor receptor bound protein 2 and phosphotyrosine-containing p...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Affinity DataIC50: 500nMAssay Description:Antagonist activity at rat TRPV1 expressed in Xenopus laevis oocytes assessed as blockage of capsaicin-induced current at holding potential -60 mV by...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Affinity DataIC50: 550nMAssay Description:Antagonist activity at rat TRPV1 expressed in Xenopus laevis oocytes assessed as blockage of capsaicin-induced current at holding potential -60 mV by...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Affinity DataIC50: 660nMAssay Description:Antagonist activity at rat TRPV1 expressed in Xenopus laevis oocytes assessed as blockage of capsaicin-induced current at holding potential -60 mV by...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Affinity DataIC50: 670nMAssay Description:Antagonist activity at rat TRPV1 expressed in Xenopus laevis oocytes assessed as blockage of capsaicin-induced current at holding potential -60 mV by...More data for this Ligand-Target Pair
Affinity DataIC50: 690nMAssay Description:Inhibition of recombinant human SIRT1 (193 to 741 residues) expressed in Escherichia coli expression system using RHKK(Ac)W-NH2 as substrate measured...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Affinity DataIC50: 840nMAssay Description:Antagonist activity at rat TRPV1 expressed in Xenopus laevis oocytes assessed as blockage of capsaicin-induced current at holding potential -60 mV by...More data for this Ligand-Target Pair
Affinity DataIC50: 930nMAssay Description:Inhibition of recombinant human SIRT2 expressed in baculovirus infected SF9 cells expression system using RHKK(Ac)W-NH2 as substrate measured after 2...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Affinity DataIC50: 960nMAssay Description:Antagonist activity at rat TRPV1 expressed in Xenopus laevis oocytes assessed as blockage of capsaicin-induced current at holding potential -60 mV by...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Affinity DataIC50: 970nMAssay Description:Antagonist activity at rat TRPV1 expressed in Xenopus laevis oocytes assessed as blockage of capsaicin-induced current at holding potential -60 mV by...More data for this Ligand-Target Pair
Affinity DataIC50: 1.10E+3nMAssay Description:The compound was evaluated for its potency to inhibit the interaction between Growth factor receptor bound protein 2 and phosphotyrosine-containing p...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Affinity DataIC50: 1.20E+3nMAssay Description:Antagonist activity at rat TRPV1 expressed in Xenopus laevis oocytes assessed as blockage of capsaicin-induced current at holding potential -60 mV by...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Affinity DataIC50: 1.21E+3nMAssay Description:Antagonist activity at rat TRPV1 expressed in Xenopus laevis oocytes assessed as blockage of capsaicin-induced current at holding potential -60 mV by...More data for this Ligand-Target Pair
Affinity DataIC50: 1.50E+3nMAssay Description:Inhibition of recombinant human SIRT2 expressed in baculovirus infected SF9 cells expression system using RHKK(Ac)W-NH2 as substrate measured after 2...More data for this Ligand-Target Pair
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibition of recombinant human SIRT1 (193 to 741 residues) expressed in Escherichia coli expression system using RHKK(Ac)W-NH2 as substrate measured...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Affinity DataIC50: 1.63E+3nMAssay Description:Antagonist activity at rat TRPV1 expressed in Xenopus laevis oocytes assessed as blockage of capsaicin-induced current at holding potential -60 mV by...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Affinity DataIC50: 2.33E+3nMAssay Description:Antagonist activity at rat TRPV1 expressed in Xenopus laevis oocytes assessed as blockage of capsaicin-induced current at holding potential -60 mV by...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Affinity DataIC50: 2.62E+3nMAssay Description:Antagonist activity at rat TRPV1 expressed in Xenopus laevis oocytes assessed as blockage of capsaicin-induced current at holding potential -60 mV by...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Affinity DataIC50: 3.06E+3nMAssay Description:Antagonist activity at rat TRPV1 expressed in Xenopus laevis oocytes assessed as blockage of capsaicin-induced current at holding potential -60 mV by...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Affinity DataIC50: 3.30E+3nMAssay Description:Antagonist activity at rat TRPV1 expressed in Xenopus laevis oocytes assessed as blockage of capsaicin-induced current at holding potential -60 mV by...More data for this Ligand-Target Pair
Affinity DataIC50: 4.20E+3nMAssay Description:Inhibition of recombinant human SIRT1 (193 to 741 residues) expressed in Escherichia coli expression system using RHKK(Ac)W-NH2 as substrate measured...More data for this Ligand-Target Pair
Affinity DataIC50: 4.90E+3nMAssay Description:Inhibition of recombinant human SIRT1 (193 to 741 residues) expressed in Escherichia coli expression system using RHKK(Ac)W-NH2 as substrate measured...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Affinity DataIC50: 4.98E+3nMAssay Description:Antagonist activity at rat TRPV1 expressed in Xenopus laevis oocytes assessed as blockage of capsaicin-induced current at holding potential -60 mV by...More data for this Ligand-Target Pair
Affinity DataIC50: 5.50E+3nMAssay Description:Inhibition of recombinant human SIRT1 (193 to 741 residues) expressed in Escherichia coli expression system using RHKK(Ac)W-NH2 as substrate measured...More data for this Ligand-Target Pair
Affinity DataIC50: 5.50E+3nMAssay Description:Inhibition of recombinant human SIRT1 (193 to 741 residues) expressed in Escherichia coli expression system using RHKK(Ac)W-NH2 as substrate measured...More data for this Ligand-Target Pair
Affinity DataIC50: 6.00E+3nMAssay Description:Inhibition of recombinant human SIRT1 (193 to 741 residues) expressed in Escherichia coli expression system using RHKK(Ac)W-NH2 as substrate measured...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Affinity DataIC50: 6.14E+3nMAssay Description:Antagonist activity at rat TRPV1 expressed in Xenopus laevis oocytes assessed as blockage of capsaicin-induced current at holding potential -60 mV by...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Affinity DataIC50: 6.40E+3nMAssay Description:Antagonist activity at rat TRPV1 expressed in Xenopus laevis oocytes assessed as blockage of capsaicin-induced current at holding potential -60 mV by...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Affinity DataIC50: 6.70E+3nMAssay Description:Antagonist activity at rat TRPV1 expressed in Xenopus laevis oocytes assessed as blockage of capsaicin-induced current at holding potential -60 mV by...More data for this Ligand-Target Pair
Affinity DataIC50: 6.80E+3nMAssay Description:Inhibition of recombinant human SIRT1 (193 to 741 residues) expressed in Escherichia coli expression system using RHKK(Ac)W-NH2 as substrate measured...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Affinity DataIC50: 7.00E+3nMAssay Description:Antagonist activity at rat TRPV1 expressed in Xenopus laevis oocytes assessed as blockage of capsaicin-induced current at holding potential -60 mV by...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Affinity DataIC50: 7.05E+3nMAssay Description:Antagonist activity at rat TRPV1 expressed in Xenopus laevis oocytes assessed as blockage of capsaicin-induced current at holding potential -60 mV by...More data for this Ligand-Target Pair
Affinity DataIC50: 7.60E+3nMAssay Description:Inhibition of recombinant human SIRT1 (193 to 741 residues) expressed in Escherichia coli expression system using RHKK(Ac)W-NH2 as substrate measured...More data for this Ligand-Target Pair
Affinity DataIC50: 9.00E+3nMAssay Description:Inhibition of human recombinant GST-fused SIRT1 expressed in Escherichia coli DH5-alpha using [3H]acetic acid labeled MPSDKTIGG as substrate after ov...More data for this Ligand-Target Pair
TargetVascular endothelial growth factor receptor 1(Homo sapiens (Human))
Umr 8638 Cnrs
Curated by ChEMBL
Umr 8638 Cnrs
Curated by ChEMBL
Affinity DataIC50: 1.04E+4nMAssay Description:Displacement of biotinylated VEGF-A (165 residues) from humanized recombinant C-terminal His-tagged VEGFR-1 extracellular domain expressed in baculov...More data for this Ligand-Target Pair
Affinity DataIC50: 1.40E+4nMAssay Description:Inhibition of recombinant human SIRT1 (193 to 741 residues) expressed in Escherichia coli expression system using RHKK(Ac)W-NH2 as substrate measured...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Institut De Qu£Mica Avan£Ada De Catalunya
Curated by ChEMBL
Affinity DataIC50: 1.86E+4nMAssay Description:Antagonist activity at rat TRPV1 expressed in Xenopus laevis oocytes assessed as blockage of capsaicin-induced current at holding potential -60 mV by...More data for this Ligand-Target Pair
TargetVascular endothelial growth factor receptor 1(Homo sapiens (Human))
Umr 8638 Cnrs
Curated by ChEMBL
Umr 8638 Cnrs
Curated by ChEMBL
Affinity DataIC50: 1.93E+4nMAssay Description:Displacement of biotinylated VEGF165 from human recombinant VEGFR1 by chemiluminescent assayMore data for this Ligand-Target Pair
TargetVascular endothelial growth factor receptor 1(Homo sapiens (Human))
Umr 8638 Cnrs
Curated by ChEMBL
Umr 8638 Cnrs
Curated by ChEMBL
Affinity DataIC50: 1.94E+4nMAssay Description:Displacement of biotinylated VEGF165 from human recombinant VEGFR1More data for this Ligand-Target Pair
Affinity DataIC50: 2.20E+4nMAssay Description:Inhibition of human recombinant GST-fused SIRT2 expressed in Escherichia coli DH5-alpha using [3H]acetic acid labeled MPSDKTIGG as substrate after ov...More data for this Ligand-Target Pair